Drug discovery of anticancer drugs targeting methylenetetrahydrofolate dehydrogenase 2

被引:24
|
作者
Asai, Ayumu [1 ,2 ,3 ]
Koseki, Jun [1 ]
Konno, Masamitsu [2 ]
Nishimura, Tatsunori [4 ]
Gotoh, Noriko [4 ]
Satoh, Taroh [2 ]
Doki, Yuichiro [1 ,2 ,3 ]
Mori, Masaki [1 ,2 ,3 ,5 ]
Ishii, Hideshi [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Med Data Sci, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Frontier Sci Canc & Chemotherapy, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Med, Dept Gastroenterol Surg, Suita, Osaka 5650871, Japan
[4] Kanazawa Univ, Canc Res Inst, Div Canc Cell Biol, Kanazawa, Ishikawa 9201192, Japan
[5] Kyushu Univ, Grad Sch Med Sci, Dept Surg & Sci, Fukuoka, Fukuoka 8128582, Japan
来源
HELIYON | 2018年 / 4卷 / 12期
关键词
Cancer research; Pharmaceutical science; Molecular biology;
D O I
10.1016/j.heliyon.2018.e01021
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many anticancer drugs have serious adverse effects; therefore, it is necessary to target features specific to cancer cells to minimize the effects on healthy cells. Methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) was reported to be specifically enhanced in cancer. We confirmed the validity of MTHFD2 as a drug discovery target using clinical data. In addition, we performed in silico screening to design an anticancer drug specifically targeting MTHFD2. Analysis of the clinical data indicated that MTHFD2 was enhanced in most cancers compared with normal tissues, and affected the prognosis in cancer patients. Candidate compounds for MTHFD2 inhibitors were identified using in silico drug discovery techniques, and the important interactions for MTHFD2 binding were determined. In addition, these candidate compounds decreased levels of MTHFD2 metabolites in cancer cells. The findings of the present study may help to develop anticancer drugs targeting MTHFD2, with a view to minimizing the adverse effects of anticancer drugs.
引用
收藏
页数:17
相关论文
共 50 条
  • [21] Anticancer drug discovery and development
    Colotta, Francesco
    TARGETED THERAPIES IN CANCER: MYTH OR REALITY?, 2008, 610 : 19 - 42
  • [22] Novel anticancer drug discovery
    Buolamwini, JK
    CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (04) : 500 - 509
  • [23] Targeting SV2A for discovery of antiepileptic drugs
    Kaminski, Rafal M.
    Gillard, Michel
    Klitgaard, Henrik
    EPILEPSIA, 2010, 51 : 83 - 83
  • [24] Progress in the discovery of biosynthetic anticancer drugs
    Pettit, GR
    JOURNAL OF NATURAL PRODUCTS, 1996, 59 (08): : 812 - 821
  • [25] Discovery of the combretastatin anticancer drugs.
    Pettit, GR
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2001, 221 : U1 - U1
  • [27] Development of novel inhibitors targeting HIF-1α towards anticancer drug discovery
    Yewalkar, Nilambari
    Deore, Vijaykumar
    Padgaonkar, Amol
    Manohar, Sonal
    Sahu, Bichismita
    Kumar, Pramod
    Jalota-Badhwar, Archana
    Joshi, Kalpana S.
    Sharma, Somesh
    Kumar, Sanjay
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (22) : 6426 - 6429
  • [28] Repurposing anticancer drugs for targeting necroptosis
    Fulda, Simone
    CELL CYCLE, 2018, 17 (07) : 829 - 832
  • [29] ANTICANCER DRUGS Selectively targeting turnover
    Barry, Isobel
    NATURE REVIEWS DRUG DISCOVERY, 2009, 8 (06) : 453 - 453
  • [30] Temporal sequencing of anticancer drugs, ex vivo, optimizes therapeutic effect by targeting drug-induced glucose-6-phosphate dehydrogenase
    Ulaganathan, Baraneedharan
    Dhawan, Andrew
    Majumder, Biswanath
    Smalley, Munisha
    Thiyagarajan, Saravanan
    Kodaganur, Gopinath S.
    Krishnamurthy, S.
    Rahman, Mohammed Mamunur
    Freinkman, Elizaveta
    Majumder, Pradip
    Kohandel, Mohammad
    Goldman, Aaron
    CANCER RESEARCH, 2018, 78 (13)